Westwood Andrew J, Beiser Alexa, Jain Nikita, Himali Jayandra J, DeCarli Charles, Auerbach Sanford H, Pase Matthew P, Seshadri Sudha
From the Department of Neurology (A.J.W., A.B., J.J.H., S.H.A., M.P.P., S.S.), Boston University School of Medicine; Department of Biostatistics (A.B., J.J.H.), Boston University School of Public Health; Framingham Heart Study (A.B., J.J.H., S.H.A., M.P.P., S.S.); Department of Neuroscience (N.J.), Boston University, MA; University of California at Davis (C.D.), Sacramento; and Center for Human Psychopharmacology (M.P.P.), Swinburne University of Technology, Australia.
Neurology. 2017 Mar 21;88(12):1172-1179. doi: 10.1212/WNL.0000000000003732. Epub 2017 Feb 22.
To evaluate the association between sleep duration and the risk of incident dementia and brain aging.
Self-reported total hours of sleep were examined in the Framingham Heart Study (n = 2,457, mean age 72 ± 6 years, 57% women) as a 3-level variable: <6 hours (short), 6-9 hours (reference), and >9 hours (long), and was related to the risk of incident dementia over 10 years, and cross-sectionally to total cerebral brain volume (TCBV) and cognitive performance.
We observed 234 cases of all-cause dementia over 10 years of follow-up. In multivariable analyses, prolonged sleep duration was associated with an increased risk of incident dementia (hazard ratio [HR] 2.01; 95% confidence interval [CI] 1.24-3.26). These findings were driven by persons with baseline mild cognitive impairment (HR 2.83; 95% CI 1.06-7.55) and persons without a high school degree (HR 6.05; 95% CI 3.00-12.18). Transitioning to sleeping >9 hours over a mean period of 13 years before baseline was associated with an increased risk of all-cause dementia (HR 2.43; 95% CI 1.44-4.11) and clinical Alzheimer disease (HR 2.20; 95% CI 1.17-4.13). Relative to sleeping 6-9 hours, long sleep duration was also associated cross-sectionally with smaller TCBV (β ± SE, -1.08 ± 0.41 mean units of TCBV difference) and poorer executive function (β ± SE, -0.41 ± 0.13 SD units of Trail Making Test B minus A score difference).
Prolonged sleep duration may be a marker of early neurodegeneration and hence a useful clinical tool to identify those at a higher risk of progressing to clinical dementia within 10 years.
评估睡眠时间与新发痴呆症风险及脑老化之间的关联。
在弗雷明汉心脏研究中(n = 2457,平均年龄72±6岁,57%为女性),将自我报告的总睡眠时间作为一个三级变量进行检查:<6小时(短)、6 - 9小时(参照)和>9小时(长),并将其与10年内新发痴呆症的风险相关联,同时与全脑脑容量(TCBV)和认知表现进行横断面分析。
在10年的随访中,我们观察到234例全因性痴呆病例。在多变量分析中,睡眠时间延长与新发痴呆症风险增加相关(风险比[HR] 2.01;95%置信区间[CI] 1.24 - 3.26)。这些发现主要由基线时患有轻度认知障碍的人群(HR 2.83;95% CI 1.06 - 7.55)和未获得高中学历的人群(HR 6.05;95% CI 3.00 - 12.18)驱动。在基线前平均13年的时间里转变为睡眠时间>9小时与全因性痴呆风险增加相关(HR 2.43;95% CI 1.44 - 4.11)以及临床阿尔茨海默病风险增加相关(HR 2.20;95% CI 1.17 - 4.13)。相对于睡眠时间为6 - 9小时,长睡眠时间在横断面上也与较小的TCBV相关(β±SE,-1.08±0.41个TCBV差异平均单位)以及较差的执行功能相关(β±SE,-0.41±0.13个连线测验B减去A得分差异的标准差单位)。
睡眠时间延长可能是早期神经退行性变的一个标志,因此是一种有用的临床工具,可用于识别在10年内进展为临床痴呆症风险较高的人群。